Canonical Allele Identifier: CA6353992

Gene: FOXRED1

Linked Data

• dbSNP Id: rs775430669
• ExAC: 11:126141406 C / CA
• gnomAD v2: 11-126141406-C-CA
• gnomAD v4: 11-126271511-C-CA
• MyVariant Identifiers: chr11:g.126141406_126141407insA (hg19) ; chr11:g.126271511_126271512insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271513dup , CM000673.2:g.126271513dup	GRCh38
NC_000011.9:g.126141408dup , CM000673.1:g.126141408dup	GRCh37
NC_000011.8:g.125646618dup	NCBI36
NG_028029.1:g.7474dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.340dup
ENST00000532101.6:n.339dup
ENST00000532125.2:c.162dup	ENSP00000434178.2:p.Asp55ArgfsTer?
ENST00000533839.6:c.85+2222dup	ENSP00000509952.1:n.85+2222dup
ENST00000534011.6:n.438dup
ENST00000685484.1:c.162dup	ENSP00000510622.1:p.Asp55ArgfsTer?
ENST00000685601.1:c.162dup	ENSP00000510603.1:p.Asp55ArgfsTer?
ENST00000685765.1:c.162dup	ENSP00000509991.1:p.Asp55ArgfsTer?
ENST00000685844.1:c.86-1456dup	ENSP00000509820.1:n.86-1456dup
ENST00000685857.1:n.340dup
ENST00000686242.1:c.86-1456dup	ENSP00000508950.1:n.86-1456dup
ENST00000686888.1:c.162dup	ENSP00000509619.1:p.Asp55ArgfsTer?
ENST00000687699.1:c.286dup	ENSP00000508878.1:n.286dup
ENST00000687786.1:n.1495dup
ENST00000688588.1:c.162dup	ENSP00000510802.1:p.Asp55ArgfsTer?
ENST00000688927.1:n.340dup
ENST00000689283.1:c.210-1456dup	ENSP00000509050.1:n.210-1456dup
ENST00000689477.1:c.*55dup	ENSP00000508945.1:n.*55dup
ENST00000689765.1:c.86-1456dup	ENSP00000509625.1:n.86-1456dup
ENST00000690512.1:c.86-965dup	ENSP00000509793.1:n.86-965dup
ENST00000692039.1:c.248dup	ENSP00000508821.1:p.Thr84AspfsTer?
ENST00000692336.1:c.162dup	ENSP00000508540.1:p.Asp55ArgfsTer?
ENST00000693133.1:n.226-1456dup
ENST00000263578.10:c.162dup MANE Select	ENSP00000263578.5:p.Asp55ArgfsTer?
ENST00000263578.9:c.162dup	ENSP00000263578.5:p.Asp55ArgfsTer?
ENST00000524751.5:n.223-1456dup
ENST00000525083.5:n.122-1456dup
ENST00000525770.5:c.86-1456dup	ENSP00000434739.1:n.86-1456dup
ENST00000526366.5:n.101-206dup
ENST00000526525.1:n.246-1456dup
ENST00000527004.5:c.162dup	ENSP00000436374.1:p.Asp55ArgfsTer?
ENST00000529802.1:n.212dup
ENST00000532101.5:n.385dup
ENST00000532125.1:c.120dup	ENSP00000434178.1:p.Asp41ArgfsTer?
ENST00000533839.5:n.237+2222dup
ENST00000534011.5:n.158-965dup
ENST00000534315.5:n.569dup
NM_017547.3:c.162dup	NP_060017.1:p.Asp55ArgfsTer?
NR_037647.1:n.253-1456dup
NR_037648.1:n.348dup
XM_006718880.2:c.-377dup	XP_006718943.1:n.-377dup
XM_006718881.2:c.-232-1456dup	XP_006718944.1:n.-232-1456dup
XM_011542895.1:c.-349dup	XP_011541197.1:n.-349dup
XM_011542896.1:c.-369dup	XP_011541198.1:n.-369dup
XM_006718881.3:c.-232-1456dup	XP_006718944.1:n.-232-1456dup
XM_011542895.2:c.-349dup	XP_011541197.1:n.-349dup
XM_011542896.2:c.-369dup	XP_011541198.1:n.-369dup
XM_017018000.2:c.162dup	XP_016873489.1:p.Asp55ArgfsTer?
XM_017018001.1:c.-369dup	XP_016873490.1:n.-369dup
XM_017018002.1:c.-224-1456dup	XP_016873491.1:n.-224-1456dup
XM_017018003.2:c.-377dup	XP_016873492.1:n.-377dup
XM_017018004.1:c.-377dup	XP_016873493.1:n.-377dup
XM_017018005.1:c.-575dup	XP_016873494.1:n.-575dup
XM_017018006.2:c.-377dup	XP_016873495.1:n.-377dup
NM_017547.4:c.162dup MANE Select	NP_060017.1:p.Asp55ArgfsTer?
NR_037647.2:n.139-1456dup
NR_037648.2:n.339dup